受体

SDS-PAGE and Western blot of culture supernatant showed that hsIL-1RⅠ was secretively expressed. Recptor-ligand binding assays showed that the recombinant hsIL-1RⅠ has receptorligand binding activity.

发酵液经SDS-PAGE和Western blot证实分泌表达了sIL-1RI，经蛋白印迹受体配基结合反应证实分泌表达的sIL-1RI具有配基受体结合的生物学活性。

The present study was performed to investigated the effects of sex hormones on the cell proliferation and differentiation of embryonic chick pituitary cells and peripheral neurons in vivo and in vitro, we injected specific corresponding receptor inhibitor in vivo to investigate the related mechanisms of sex hormones on the peripheral neurons.

本研究通过体内实验、体外实验研究了性激素对鸡胚垂体细胞和鸡胚外周神经元的增殖、分化的调节功能，通过在体注射性激素受体的特异抑制剂来研究性激素对外周神经元作用的相关机理，并通过检测鸡胚和绵羊胚胎垂体发育过程中雌激素受体的变化对雌激素调节内分泌细胞的作用机理进行了比较研究。

Other studies in Caucasian population found that endogenous sex hormone and ER and PR were associated with breast cancer.

也有研究认为内源性性激素的暴露联合肿瘤的雌激素受体和孕激素受体状态与乳腺癌的发病有关。

Further study indicated that HI117 and SJ9A4-induced Fg binding was reduced by pretreatment of platelets with sphingosine, aspirin, apyrase, and/or PGI2. Conclusion The anti-CD9 McAbs, HI117 and SJ9A4, can reversibly expose platelet Fg receptors, probably via three signaling pathways, i.e.

HI117和SJ9A4均能诱发血小板膜Fg受体暴露，两者诱发人血小板Fg受体暴露可能是三条途径综合作用的结果：即二磷酸腺苷释放、血栓烷生成和环磷酸腺苷途径，而PKC激活可能是三条途径的共同通路。

In addition,weak mGluR7-LI was detected in some other regions of the brain and spinal cord.

而受体蛋白的定位研究对了解受体的功能是不可缺少的。

Methods NPE models of rabbits were made and H1 receptor antagonist (chlorpheniramine, H1 group), H2 receptor antagonist (Cimetidine, H2 group) or normal sodium were injected into PVN of rabbits utilizing the technique of stereotaxis. The degree of pulmonary edema was observed, the content of histamine in PVN was measured by high performance liquid chromatogram, and the ration of lung-water and A/P value were calculated.

制作家兔NPE模型；座用中枢立体定位技术，在家兔PVN微量注射组胺H1受体拮抗剂（扑尔敏，H1组）、H2受体拮抗剂（西米替丁，H2组）及生理盐水，现察肺水肿程度，高效液相法检测各组家兔PVN内组胺含量，测定肺水比、肺水肿液中蛋白含量与血浆蛋白含量的比值。

Novel compounds of the structural formula are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor.

结构式化合物是大麻素-1(CB1)受体的拮抗剂和/或反向激动剂，可用于治疗、预防和抑制CB1受体介导的疾病。

B Submaxillary can synthesize GnRH receptor, GnRH regulate the physiological function of submaxillary through autocrine or paracrine mechanism.

颌下腺能自身合成GnRH受体，受体的分布也和先前研究的GnRH相一致，说明GnRH可通过自分泌和／或旁分泌的机制调节颌下腺的生理功能

C The cDNA sequence of GnRH receptor in submaxillary is identical to the relative sequence of GnRH receptor in pituitary, but whether the entire sequence of GnRH receptor are identical between two organs should be further studied.

颌下腺GnRH受体cDNA序列和大鼠脑垂体的GnRH受体的相应片段相同，但全长序列是否相同，尚无定论。4.GnRH具有调节大鼠颌下腺分泌NGF的作用。

Estrogen receptor is one of the members of the nuclear receptor superfamily, and contains two subtypes: a and p.

雌激素受体是核受体超级家族成员之一，它包括两种亚型：α和β。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！